# Investigation of ER-endosome contact site dysfunction underlying pathomechanism of hereditary spastic paraplegia > **NIH NIH F32** · YALE UNIVERSITY · 2020 · $67,446 ## Abstract Broadly, the goal of this application is to understand how ER-endosome contact site dysfunction underlies the pathomechanisms of hereditary spastic paraplegia (HSP). Membrane contact sites (MCS) form between the endoplasmic reticulum (ER) and endosomes/lysosomes to facilitate processes such as fission, receptor dephosphorylation, and lipid exchange. Contact sites specifically with late endosomes (LE) have been observed to govern vesicular positioning and cholesterol transfer to the ER additionally. Mammalian cells have been reported to form contact sites with the ER and 99% of LEs. Most LEs will undergo fusion with the lysosome, completing their endocytic life-cycle. However, a mobile subset traffic directionally to the PM in response to protrusion demand. Recent efforts have focused on understanding how the formation of MCS with LEs is initiated and how observed changes in vesicular mobility occur. To date, how MCS mediate the increasing mobility of LEs in response to protrusion demand remains poorly understood. Recent investigation has uncovered novel regulatory functions of ER/endosome MCS during neurodevelopment, including protrusion and neurite outgrowth. I aim to understand how mutations in proteins responsible for mediating MCS impair neurite outgrowth. Specifically, I seek to characterize the transitional forces of the ER-resident protein Protrudin using single-molecule force spectroscopy. Several Protrudin effectors and interacting partners may alter MCS organization in mammalian cells, including the well-known VAP homologs. Protrudin has been implicated in the initiation of late endosome mobility required for protrusion. However, this process is poorly understood. By measuring the forces necessary for MCS formation and endosome release, I will gain insight into how neurons select endosomes and subsequently direct vesicular trafficking during development. I also aim to use optogenetic imaging to artificially generate ER/endosome MCS during neurite outgrowth to delineating mechanisms responsible for vesicular mobility. HSPs are characterized by spastic progressive paralysis of the lower limbs through length dependent distal axonopathy of the cortical spinal tract, consistent with neurite outgrowth deficits. A missense mutation (p.G191V) in the membrane anchoring hairpin domain of Protrudin causes a dominant form of hereditary spastic paraplegia (HSP). This project emphasizes the generation of genome edited spinal motor neurons to study HSP and model the effects of ER-endosome MCS dysfunction during neurodevelopment. Using these motor neurons edited to express the mutant Protrudin at endogenous levels, I will examine the sub- cellular morphology using FIB-SEM to determine the impact on ER/endosome MCS. My project aims to build a detailed understanding of how Protrudin increases vesicular mobility. This represents an essential step in our understanding of the link between ER-endosome/lysosome MCS regulation and neurodegeneration. This award... ## Key facts - **NIH application ID:** 9951124 - **Project number:** 5F32NS108448-03 - **Recipient organization:** YALE UNIVERSITY - **Principal Investigator:** Michael George Hanna - **Activity code:** F32 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2020 - **Award amount:** $67,446 - **Award type:** 5 - **Project period:** 2018-08-01 → 2021-07-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/9951124 ## Citation > US National Institutes of Health, RePORTER application 9951124, Investigation of ER-endosome contact site dysfunction underlying pathomechanism of hereditary spastic paraplegia (5F32NS108448-03). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/9951124. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*